APPEAL ANTIBACTERIAL HAND WASH- benzalkonium chloride solution 
SC Johnson Professional USA, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredient

BENZALKONIUM CHLORIDE, 0.13%

Purpose

Antibacterial

Uses

for handwashing to reduce bacteria on the skin

Warnings

For external use only

When using this product

avoid contact with eyes. In case of eye contact, flush with water.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

apply foaming cleanser to dry hands
rub hands together to spread lather
wash for 15-20 seconds
rinse & dry hands thoroughly

Inactive ingredients

AQUA (WATER), GLYCERIN, LAURAMINE OXIDE, BUTYLENE GLYCOL, LACTIC ACID, SALICYLIC ACID, PARFUM (FRAGRANCE), GREEN 5 (CI 61570), YELLOW 5 (CI 19140).

APP17201-04-R00-Appeal Antibac Hand Wash 1L-V12.jpg

APP17201-04

3577410

appeal

Antibacterial Hand Wash

deb

Made in the USA by Deb

1 L (33.8 fl oz)

Distributed exclusively by:

Interline Brands

Jacksonville, FL 32207

www.AppealProducts.com

R00

APPEAL ANTIBACTERIAL HAND WASH 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-015
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)  
SALICYLIC ACID (UNII: O414PZ4LPZ)  
D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11084-015-271000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/12/2017
2NDC:11084-015-661000 mL in 1 BOTTLE; Type 0: Not a Combination Product02/17/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/12/2017
Labeler - SC Johnson Professional USA, Inc. (607378015)
Establishment
NameAddressID/FEIBusiness Operations
APEX International, Inc.015226132MANUFACTURE(11084-015)

Revised: 2/2023
Document Id: a1120e4f-ddcc-4b98-b6dd-024a8679261f
Set id: 357a4349-76f5-47b8-ae72-b1dbe1993886
Version: 3
Effective Time: 20230227
 
SC Johnson Professional USA, Inc.